Medical Director

Parexel; Ourense; Híbrido; EUR 90.000 - 130.000; Jornada completa

Descripción de la vacante

Parexel seeks a Medical Director with a strong background in Ophthalmology to enhance medical monitoring and client engagement for biopharmaceutical projects. This role emphasizes expertise in drug development and excellent communication skills, focusing on building relationships and supporting clinical trials. The position offers flexibility in select EMEA locations.

Formación

• Specialty in Ophthalmology with up-to-date qualifications.
• Experience in drug development and medical monitoring preferred.
• Leadership experience in managing teams is beneficial.

Responsabilidades

• Deliver all medical support required for project delivery.
• Build and maintain client relationships.
• Provide medical expertise in proposal development for client bid pursuits.

Conocimientos

Interpersonal skills

Client-focused approach

Verbal and written medical communication

Excellent English

Flexibility

Task management skills

Teamwork

Educación

Medically qualified from an acknowledged medical school

Completion of residency or internship

Descripción del empleo

When our values align, there's no limit to what we can achieve.

Parexel is in the business of improving the world's health. We do this by providing a suite of biopharmaceutical services that help clients across the globe transform scientific discoveries into new treatments. From clinical trials to regulatory, consulting, and market access, our therapeutic, technical, and functional ability is underpinned by a deep conviction in what we do. We believe in our values : Patients First, Quality, Respect, Empowerment & Accountability.

Parexel is looking for a Medical Director with a very strong background in Ophthalmology.

The role can be based remotely in select EMEA locations.

The Medical Director is a medical expert with specialized therapeutic expertise and some experience across indications, clients, and drug development. They initiate and maintain medical and consultative relationships with clients, consult on early engagement and pre-award efforts, and serve as a medical monitor for contracted projects. The Medical Director may take on leadership roles by participating in initiatives, mentoring junior MDs, and / or managing a team of physicians where appropriate.

Primary activities will focus on Medical Monitoring Delivery & PV Support. The medical monitor will independently deliver all medical support required for successful project delivery according to the contracted agreement with the sponsor (i.e., tasks and time per task contracted) and according to the assigned role (Global Lead Physician or Regional Lead Physician).

Medical expertise and experience in Ophthalmology are essential for the medical monitor role and will be demonstrated through high-quality consultation on protocol development or drug development programs, medical review of various documents, collaboration on internal therapeutic area meetings, training module development, white papers, slide sets, publications, etc.

Client relationship building & engagement, including soliciting and addressing client feedback and suggestions regarding medical study-related activities, are core skills required of the medical monitor.

Business development : the medical monitor will provide medical expertise and leadership in Proposal Development Teams (PDTs) for client bid pursuit meetings.

Skills

• Excellent interpersonal skills, including the ability to interact well with sponsor / client counterparts
• Client-focused approach to work
• Excellent verbal and written medical communication skills
• Excellent standard of written and spoken English
• A flexible attitude with respect to work assignments and new learning
• Ability to manage multiple and varied tasks with enthusiasm and prioritize workload with attention to detail
• Willingness to work in a matrix environment and to value the importance of teamwork

Knowledge And Experience

• Experience in clinical medicine (general or specialist qualifications) with a specialty in Ophthalmology, which is expected to be kept up to date.
• A background in clinical aspects of drug development, including all aspects of Medical Monitoring and study design / execution, is preferred.
• Clinical practice experience
• Good knowledge of the drug development process, including drug safety, is preferred.
• Experience in Pharmaceutical Medicine is preferred.
• Experience leading, mentoring, and managing individuals or a team is preferred.

Education

• Medically qualified in an acknowledged medical school with completion of at least basic training in clinical medicine (residency, internship).

J-18808-Ljbffr

J-18808-Ljbffr